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92978002: Congenital absence of thyroid gland (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
153761017 Congenital absence of thyroid gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510170019 Congenital thyroid aplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836614015 Congenital absence of thyroid gland (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
153761017 Congenital absence of thyroid gland en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
153761017 Congenital absence of thyroid gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510169015 Aplasia of thyroid with myxedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
510169015 Aplasia of thyroid with myxedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510170019 Congenital thyroid aplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
510170019 Congenital thyroid aplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510171015 Aplasia of thyroid with myxoedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
510171015 Aplasia of thyroid with myxoedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836614015 Congenital absence of thyroid gland (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836614015 Congenital absence of thyroid gland (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4705411000241110 absence thyroïdienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4705411000241110 absence thyroïdienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of thyroid gland Is a Congenital anomaly of the thyroid gland true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of thyroid gland Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of thyroid gland Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of thyroid gland Finding site Thyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of thyroid gland Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of thyroid gland Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of thyroid gland Is a Congenital absence false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of thyroid gland Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of thyroid gland Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of thyroid gland Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Is a True Congenital absence of thyroid gland Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypothyroidism due to absence of thyroid gland (disorder) Due to True Congenital absence of thyroid gland Inferred relationship Existential restriction modifier (core metadata concept) 3

Reference Sets

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